Molecular docking, DFT studies, and anti-inflammatory evaluation of peshawaraquinone isolated from Fernandoa adenophylla

被引:0
|
作者
AlOmar, Taghrid S. [1 ]
Rauf, Abdur [1 ,2 ]
Rashid, Umer [3 ]
Sarfaraz, Sehrish [3 ]
Ayub, Khurshid [3 ]
Hussain, Fahad [3 ]
Almasoud, Najla [1 ]
AlOmar, Abdulaziz S. [4 ]
Rehman, Gauhar [5 ]
Ahmad, Zubair [2 ]
Muhammad, Naveed [6 ]
Ali Shah, Zafar [7 ]
机构
[1] Princess Nourah Bint Abdulrahman Univ, Coll Sci, Dept Chem, POB 84427, Riyadh 11671, Saudi Arabia
[2] Univ Swabi, Dept Chem, Swabi 23561, Khyber Pakhtunk, Pakistan
[3] COMSATS Univ Islamabad, Dept Chem, Islamabad, Pakistan
[4] Al Imam Mohammad Ibn Saud Islamic Univ IMSIU, Coll Med, Riyadh, Saudi Arabia
[5] Abdul Wali Khan Univ, Dept Zool, Mardan, Pakistan
[6] Abdul Wali Khan Univ, Dept Pharm, Mardan, Pakistan
[7] Agr Univ Peshawar, Dept Agron, Peshawar, Pakistan
来源
关键词
Fernandoa adenophylla; peshawaraquinone; anti-inflammatory potential; HRBC assay; xylene-induced ear edema mode; DENSITY-FUNCTIONAL THEORY; IN-VIVO; NAPHTHOQUINONES; INFLAMMATION; DERIVATIVES; INHIBITION; LAPACHOL; DRUG;
D O I
10.1080/07391102.2023.2258402
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In recent years, there has been growing interest in exploring natural compounds with anti-inflammatory properties for potential therapeutic applications. This study focuses on investigating the anti-inflammatory potential of peshawaraquinone (PAQ), a compound isolated from Fernandoa adenophylla, which is known for its local use in pain relief. We aim to evaluate the efficacy of peshawaraquinone in both in vitro and in vivo models and gain insights into its mode of action. In the in vitro Human red blood cell (HRBC) assay, various concentrations of peshawaraquinone were tested for their ability to inhibit the hemolysis of red blood cells, a well-established indicator of anti-inflammatory activity. The results demonstrated a maximum percent inhibition of 79.69 at a concentration of 100 mu M, indicating significant anti-inflammatory potential. Furthermore, the in vivo xylene-induced ear edema model was employed to assess the compound's efficacy in reducing inflammation. Xylene was topically applied to the ear to induce edema, and peshawaraquinone was administered to evaluate its inhibitory effects. The findings revealed a sub-stantial 74.19% reduction in ear edema, accompanied by decreased ear thickness and histopathological improvements, such as inhibited cell infiltration and epidermal hyperplasia. To gain further insights into the compound's mechanism of action, density functional theory (DFT) calculations were performed to investigate its spectroscopic characteristics and geometric properties. Additionally, docking studies were conducted on key targets involved in inflammation, including COX-1 and COX-2. In conclusion, this study showcases the significant anti-inflammatory potential of peshawaraquinone, offering promising prospects for its use as a natural anti-inflammatory agent. The results from both in vitro and in vivo models, as well as the mechanistic insights gained from computational analyses, provide a solid basis for further exploration of peshawaraquinone's therapeutic applications. [GRAPHICS] .
引用
收藏
页码:10604 / 10616
页数:13
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